A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553996



Internal ID16341405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33361539..33519130hg38UCSC Ensembl
Innerchr11:33383085..33540676hg19UCSC Ensembl
Innerchr11:33339661..33497252hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38157592
hg19157592
hg18157592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174617
Samples1780854328_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553996
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer